RS1951913764 WNK1
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Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Pseudohypoaldosteronism type 2C
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Pseudohypoaldosteronism type 2C
Other Variants in WNK1